Tekin, M. Et Al. 2009. A Complex TFAP2A Allele Is Associated With Branchio-Oculo-Facial Syndrome and Inner Ear Malformation in a Deaf Child. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.149A, no.3 , 427-430.

Tekin, M., Sirmaci, A., Yuksel-Konuk, B., FİTOZ, Ö. S., & Sennaroglu, L., (2009). A Complex TFAP2A Allele Is Associated With Branchio-Oculo-Facial Syndrome and Inner Ear Malformation in a Deaf Child. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.149A, no.3, 427-430.

Tekin, Mustafa Et Al. "A Complex TFAP2A Allele Is Associated With Branchio-Oculo-Facial Syndrome and Inner Ear Malformation in a Deaf Child," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.149A, no.3, 427-430, 2009

Tekin, Mustafa Et Al. "A Complex TFAP2A Allele Is Associated With Branchio-Oculo-Facial Syndrome and Inner Ear Malformation in a Deaf Child." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.149A, no.3, pp.427-430, 2009

Tekin, M. Et Al. (2009) . "A Complex TFAP2A Allele Is Associated With Branchio-Oculo-Facial Syndrome and Inner Ear Malformation in a Deaf Child." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.149A, no.3, pp.427-430.

@article{article, author={Mustafa Tekin Et Al. }, title={A Complex TFAP2A Allele Is Associated With Branchio-Oculo-Facial Syndrome and Inner Ear Malformation in a Deaf Child}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2009, pages={427-430} }